A case report of congenital Hemangiopericytoma as a buttock mass in a newborn

Objective: Hemangiopericytoma is a rare tumor with vascular origin with an incidence of only 10% among children. Along with the report of this rare condition, we reviewed literature. Case: A full term neonate with a birth weight appropriate to gestational age referred with a posterior midline buttoc...

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Autores principales: Y ZahedPasha, M Ahmad Pour, A Hadipour, E Shafigh
Formato: article
Lenguaje:EN
FA
Publicado: Babol University of Medical Sciences 2001
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Acceso en línea:https://doaj.org/article/e2cc3d5b5c114f9583b4c3d414e29ee5
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spelling oai:doaj.org-article:e2cc3d5b5c114f9583b4c3d414e29ee52021-11-10T09:21:13ZA case report of congenital Hemangiopericytoma as a buttock mass in a newborn1561-41072251-7170https://doaj.org/article/e2cc3d5b5c114f9583b4c3d414e29ee52001-10-01T00:00:00Zhttp://jbums.org/article-1-2855-en.htmlhttps://doaj.org/toc/1561-4107https://doaj.org/toc/2251-7170Objective: Hemangiopericytoma is a rare tumor with vascular origin with an incidence of only 10% among children. Along with the report of this rare condition, we reviewed literature. Case: A full term neonate with a birth weight appropriate to gestational age referred with a posterior midline buttock mass. The tumor was resected completely, the histopathologic and immunohistochemistry reaction showed hemangiopericytoma. Regular follow up examinations after discharge showed no recurrence at the location of resection and no remote metastasis up to 11 months of age. Conclusion: Hemangiopericytoma should be considered in differential diagnosis of posterior midline buttock mass in a neonate.Y ZahedPashaM Ahmad PourA HadipourE ShafighBabol University of Medical Sciencesarticlehemangiopericytoma neonatetumorbuttock massMedicineRMedicine (General)R5-920ENFAMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 3, Iss 4, Pp 53-56 (2001)
institution DOAJ
collection DOAJ
language EN
FA
topic hemangiopericytoma neonate
tumor
buttock mass
Medicine
R
Medicine (General)
R5-920
spellingShingle hemangiopericytoma neonate
tumor
buttock mass
Medicine
R
Medicine (General)
R5-920
Y ZahedPasha
M Ahmad Pour
A Hadipour
E Shafigh
A case report of congenital Hemangiopericytoma as a buttock mass in a newborn
description Objective: Hemangiopericytoma is a rare tumor with vascular origin with an incidence of only 10% among children. Along with the report of this rare condition, we reviewed literature. Case: A full term neonate with a birth weight appropriate to gestational age referred with a posterior midline buttock mass. The tumor was resected completely, the histopathologic and immunohistochemistry reaction showed hemangiopericytoma. Regular follow up examinations after discharge showed no recurrence at the location of resection and no remote metastasis up to 11 months of age. Conclusion: Hemangiopericytoma should be considered in differential diagnosis of posterior midline buttock mass in a neonate.
format article
author Y ZahedPasha
M Ahmad Pour
A Hadipour
E Shafigh
author_facet Y ZahedPasha
M Ahmad Pour
A Hadipour
E Shafigh
author_sort Y ZahedPasha
title A case report of congenital Hemangiopericytoma as a buttock mass in a newborn
title_short A case report of congenital Hemangiopericytoma as a buttock mass in a newborn
title_full A case report of congenital Hemangiopericytoma as a buttock mass in a newborn
title_fullStr A case report of congenital Hemangiopericytoma as a buttock mass in a newborn
title_full_unstemmed A case report of congenital Hemangiopericytoma as a buttock mass in a newborn
title_sort case report of congenital hemangiopericytoma as a buttock mass in a newborn
publisher Babol University of Medical Sciences
publishDate 2001
url https://doaj.org/article/e2cc3d5b5c114f9583b4c3d414e29ee5
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